A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982202



Internal ID18617397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21420184..21420684hg38UCSC Ensembl
Innerchr9:21420183..21420683hg19UCSC Ensembl
Innerchr9:21410183..21410683hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2524527, nssv2524519, nssv2524523, nssv2524526, nssv2524524, nssv2524521, nssv2524520, nssv2524528, nssv2524525, nssv2524522
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982202
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer